Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 11:47438005 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature and has 3 sample genotypes.

Variant displays